About this trial
This prospective, randomized phase II trial is designed to evaluate whether low-dose short-course radiotherapy differs from common-dose short-course radiotherapy in terms of efficacy when both regimens are sequentially combined with CAPOX, a PD-1 monoclonal antibody, and interleukin-2 (IL-2) in patients with locally advanced rectal cancer. The study is based on findings from our previous single-center, single-arm PRIDE01 study, in which neoadjuvant short-course radiotherapy followed by systemic chemoimmunotherapy and IL-2 demonstrated encouraging antitumor activity relative to historical short-course radiotherapy-based approaches. The current trial aims to provide more robust clinical evidence regarding the potential role of low-dose radiotherapy combined with IL-2 as a sensitization strategy in multimodal neoadjuvant therapy. By comparing complete response rates between the two radiotherapy dose levels, this study may help define an optimized neoadjuvant approach and support future organ-preservation strategies for patients with locally advanced rectal cancer.
Eligibility criteria
Qualifiers
Male and female patients aged 18 to 70 years.
Histologically confirmed rectal adenocarcinoma with the distal margin of the tumor located within 12 cm of the anal verge.
MRI-based clinical stage T3-T4 or any T with lymph node-positive (N+) disease.
Adequate hematologic, hepatic, and renal function defined as: absolute neutrophil count >=1.5 x 10^9/L; platelet count >=75 x 10^9/L; serum total bilirubin <=1.5 x upper normal limit (UNL); aspartate aminotransferase <=2.5 x UNL; alanine aminotransferase <=2.5 x UNL; serum creatinine <=1.5 x UNL.
Disqualifiers
Metastatic disease (Stage IV).
Recurrent rectal cancer.
Concurrent active bleeding, perforation, or other complicated conditions requiring emergency surgery.
Prior systemic anticancer therapy for rectal cancer.
Trial design
Treatments tested in this trial
- Sintilimab + IL-2 Combined with CAPOX
- Short-course low-dose radiotherapy
- Short-course standard-dose radiotherapy